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Abstract
Citation: Ann Clin Case Rep. 2024;9(1):2705.DOI: 10.25107/2474-1655.2705
A Case Report on Primary Inflammatory Myofibroblastic Tumor of the Stomach in an Adult Female: A Comprehensive Analysis
Wen-Wei Yu, Qiong Li, Xi-Sheng Liu and Han Ge
Department of Radiology, The First Affiliated Hospital with Nanjing Medical University, China Department of General Surgery, The First Affiliated Hospital with Nanjing Medical University, China
PDF Full Text Case Report | Open Access
Abstract:
Inflammatory Myofibroblastic Tumor (IMT) is a rare mesenchymal neoplasm characterized primarily by myofibroblastic proliferation and a prominent inflammatory infiltrate, including plasma cells and lymphocytes. Although IMTs predominantly affect adolescents and can arise in various body sites, they are exceedingly rare in adults, particularly within the stomach. This report presents a case involving an adult patient who underwent surgical resection for a suspected malignant gastric tumor, which was subsequently diagnosed as an IMT on histopathological examination.
Keywords:
Inflammatory myofibroblastic tumor; Gastric; Surgical resection
Cite the Article:
Wen-Wei Yu1, Qiong Li1, Xi-Sheng Liu, Han Ge. A Case Report on Primary Inflammatory Myofibroblastic Tumor of the Stomach in an Adult Female: A Comprehensive Analysis. Ann Clin Case Rep. 2024; 9: 2705..
Journal Basic Info
- Impact Factor: 5.253*
- H-Index: 6
- ISSN: 2474-1655
- DOI: 10.25107/2474-1655
- PubMed NLM ID: 101702800
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